Product Details

SNP ID: rs4902835
Assay Type: Validated
NCBI dbSNP Submissions: NA
Location: Chr.14:70646184 on Build GRCh38
Set Membership: Validated
Context Sequence [VIC/FAM]: CCAGTTGTGCTGGGCCCCTGGGTGT[A/G]ATTTTTGCGTATCTTGTTTTCCAGG
Phenotype: MIM: 610488
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: LOC101928075 PubMed Links

Gene Details

There are no transcripts associated with this gene.

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015351.1		Intron			NP_056166.1